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  • 219511-71-4 Structure
  • Basic information

    1. Product Name: BOC-GUANIDINE
    2. Synonyms: BOC-GUANIDINE;N-BOC-GUANIDINE;Carbamic acid, (aminoiminomethyl)-, 1,1-dimethylethyl ester (9CI);tert-Butyl N-(aminoiminomethyl)carbamate;tert-butyl N-(diaMinoMethylidene)carbaMate;(Aminoiminomethyl)carbamic acid tert-butyl ester;tert-Butoxycarbonylguanidine;tert-butyl N-carbaMiMidoylcarbaMate
    3. CAS NO:219511-71-4
    4. Molecular Formula: C6H13N3O2
    5. Molecular Weight: 159.19
    6. EINECS: N/A
    7. Product Categories: N-BOC;Building Blocks;Chemical Synthesis;Guanidines;New Products for Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks
    8. Mol File: 219511-71-4.mol
    9. Article Data: 23
  • Chemical Properties

    1. Melting Point: 170-175℃
    2. Boiling Point: 259.007 °C at 760 mmHg
    3. Flash Point: 110.444 °C
    4. Appearance: White/Powder
    5. Density: 1.189 g/cm3
    6. Vapor Pressure: 0.0133mmHg at 25°C
    7. Refractive Index: 1.498
    8. Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
    9. Solubility: Soluble in most alcohols, esters (e.g., ethyl acetate), ketones
    10. PKA: 9.60±0.46(Predicted)
    11. Sensitive: Moisture Sensitive
    12. CAS DataBase Reference: BOC-GUANIDINE(CAS DataBase Reference)
    13. NIST Chemistry Reference: BOC-GUANIDINE(219511-71-4)
    14. EPA Substance Registry System: BOC-GUANIDINE(219511-71-4)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22
    3. Safety Statements: 36-60
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 219511-71-4(Hazardous Substances Data)

219511-71-4 Usage

Description

BOC-GUANIDINE, also known as N-Boc-guanidine, is a chemical compound that serves as a guanidinylating agent and is used in the synthesis of 2-aminoimidazoles. It is a white to almost white crystalline substance and is commonly utilized as a pharmaceutical intermediate.

Uses

Used in Pharmaceutical Industry:
BOC-GUANIDINE is used as a guanidinylating agent for the synthesis of various pharmaceutical compounds. Its ability to form guanidine groups makes it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
BOC-GUANIDINE is used as a key intermediate in the synthesis of 2-aminoimidazoles, which are important building blocks in the creation of various chemical compounds and materials.
Used in Research and Development:
BOC-GUANIDINE is employed in research and development settings to explore its potential applications in various fields, including pharmaceuticals, materials science, and chemical engineering. Its unique properties and reactivity make it a promising candidate for the development of innovative products and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 219511-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,5,1 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 219511-71:
(8*2)+(7*1)+(6*9)+(5*5)+(4*1)+(3*1)+(2*7)+(1*1)=124
124 % 10 = 4
So 219511-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H13N3O2/c1-6(2,3)11-5(10)9-4(7)8/h1-3H3,(H4,7,8,9,10)

219511-71-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H63206)  N-Boc-guanidine, 95%   

  • 219511-71-4

  • 1g

  • 296.0CNY

  • Detail
  • Alfa Aesar

  • (H63206)  N-Boc-guanidine, 95%   

  • 219511-71-4

  • 5g

  • 1107.0CNY

  • Detail
  • Alfa Aesar

  • (H63206)  N-Boc-guanidine, 95%   

  • 219511-71-4

  • 25g

  • 4449.0CNY

  • Detail
  • Aldrich

  • (756342)  N-Boc-guanidine  97%

  • 219511-71-4

  • 756342-1G

  • 375.57CNY

  • Detail
  • Aldrich

  • (756342)  N-Boc-guanidine  97%

  • 219511-71-4

  • 756342-5G

  • 1,243.71CNY

  • Detail

219511-71-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(diaminomethylidene)carbamate

1.2 Other means of identification

Product number -
Other names (Aminoiminomethyl)carbamic acid tert-butyl ester tert-Butoxycarbonylguanidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:219511-71-4 SDS

219511-71-4Relevant articles and documents

Downsizing of enzymes by chemical methods: arginine mimics with low pk a values increase the rates of hydrolysis of RNA model compounds

Geiger, Lars,Schmuck, Carsten,Lindgren, N. Johan V.,Baltzer, Lars,Razkin, Jesus

, p. 6722 - 6725 (2009)

-

Triazine-Based Janus G-C Nucleobase as a Building Block for Self-Assembly, Peptide Nucleic Acids, and Smart Polymers

Meena, Chhuttan L.,Singh, Dharmendra,Kizhakeetil, Bhavya,Prasad, Manasa,George, Malini,Tothadi, Srinu,Sanjayan, Gangadhar J.

, p. 3186 - 3195 (2021/02/16)

This communication reports on the utility of a triazine-based self-assembling system, reminiscent of a Janus G-C nucleobase, as a building block for developing (1) supramolecular polymers, (2) peptide nucleic acids (PNAs), and (3) smart polymers. The strategically positioned self-complementary triple H-bonding arrays DDA and AAD facilitate efficient self-assembly, leading to a linear supramolecular polymer.

Supramolecular Self-Sorting Networks using Hydrogen-Bonding Motifs

Coubrough, Heather M.,van der Lubbe, Stephanie C. C.,Hetherington, Kristina,Minard, Aisling,Pask, Christopher,Howard, Mark J.,Fonseca Guerra, Célia,Wilson, Andrew J.

supporting information, p. 785 - 795 (2019/01/04)

A current objective in supramolecular chemistry is to mimic the transitions between complex self-sorted systems that represent a hallmark of regulatory function in nature. In this work, a self-sorting network, comprising linear hydrogen motifs, was created. Selecting six hydrogen-bonding motifs capable of both high-fidelity and promiscuous molecular recognition gave rise to a complex self-sorting system, which included motifs capable of both narcissistic and social self-sorting. Examination of the interactions between individual components, experimentally and computationally, provided a rationale for the product distribution during each phase of a cascade. This reasoning holds through up to five sequential additions of six building blocks, resulting in the construction of a biomimetic network in which the presence or absence of different components provides multiple unique pathways to distinct self-sorted configurations.

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